JP6144698B2 - Hiv複製の阻害剤としての縮合三環式化合物 - Google Patents
Hiv複製の阻害剤としての縮合三環式化合物 Download PDFInfo
- Publication number
- JP6144698B2 JP6144698B2 JP2014547651A JP2014547651A JP6144698B2 JP 6144698 B2 JP6144698 B2 JP 6144698B2 JP 2014547651 A JP2014547651 A JP 2014547651A JP 2014547651 A JP2014547651 A JP 2014547651A JP 6144698 B2 JP6144698 B2 JP 6144698B2
- Authority
- JP
- Japan
- Prior art keywords
- mmol
- compound
- general procedure
- etoac
- purification
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 0 CCOC(N([C@@](C1)C11C[C@@]2([C@@](C)C2)OCC1)c1c(C(*)=O)[o]c2c1cc(-c1c[n](C)nc1)c(C)c2[C@@](C)*)=O Chemical compound CCOC(N([C@@](C1)C11C[C@@]2([C@@](C)C2)OCC1)c1c(C(*)=O)[o]c2c1cc(-c1c[n](C)nc1)c(C)c2[C@@](C)*)=O 0.000 description 9
- XIQCSACWJUJZCL-UHFFFAOYSA-N CC(C1)C11OCCC2(CC2)C1 Chemical compound CC(C1)C11OCCC2(CC2)C1 XIQCSACWJUJZCL-UHFFFAOYSA-N 0.000 description 2
- NYPYPOZNGOXYSU-UHFFFAOYSA-N Brc1cccnc1 Chemical compound Brc1cccnc1 NYPYPOZNGOXYSU-UHFFFAOYSA-N 0.000 description 1
- NZHIIDNOLFOHSG-UHFFFAOYSA-N C1C=CC=NC1 Chemical compound C1C=CC=NC1 NZHIIDNOLFOHSG-UHFFFAOYSA-N 0.000 description 1
- YNGDWRXWKFWCJY-UHFFFAOYSA-N C1C=CNC=C1 Chemical compound C1C=CNC=C1 YNGDWRXWKFWCJY-UHFFFAOYSA-N 0.000 description 1
- DWKUKQRKVCMOLP-UHFFFAOYSA-N C1CC=NCC1 Chemical compound C1CC=NCC1 DWKUKQRKVCMOLP-UHFFFAOYSA-N 0.000 description 1
- VSWICNJIUPRZIK-UHFFFAOYSA-N C1CNC=CC1 Chemical compound C1CNC=CC1 VSWICNJIUPRZIK-UHFFFAOYSA-N 0.000 description 1
- BUDQDWGNQVEFAC-UHFFFAOYSA-N C1COC=CC1 Chemical compound C1COC=CC1 BUDQDWGNQVEFAC-UHFFFAOYSA-N 0.000 description 1
- MGADZUXDNSDTHW-UHFFFAOYSA-N C1OC=CC=C1 Chemical compound C1OC=CC=C1 MGADZUXDNSDTHW-UHFFFAOYSA-N 0.000 description 1
- DXBGFEURNZURKE-KNTRCKAVSA-N CC/C(/N(CCC1OCCC1)C(OCC)=O)=C(/C(c(cc1)cnc1NC)=O)\O Chemical compound CC/C(/N(CCC1OCCC1)C(OCC)=O)=C(/C(c(cc1)cnc1NC)=O)\O DXBGFEURNZURKE-KNTRCKAVSA-N 0.000 description 1
- NEZBOWOHESBSBN-JHNVJXEBSA-N CC/N=C/C(NC(N=C1c(nc2)ccc2OC)=O)=C1OC(C)N(C)C=N Chemical compound CC/N=C/C(NC(N=C1c(nc2)ccc2OC)=O)=C1OC(C)N(C)C=N NEZBOWOHESBSBN-JHNVJXEBSA-N 0.000 description 1
- LJUAHBJQFILHLS-UHFFFAOYSA-N CC1(C)OB(c2c[n](CC3CC3)nc2)OC1(C)C Chemical compound CC1(C)OB(c2c[n](CC3CC3)nc2)OC1(C)C LJUAHBJQFILHLS-UHFFFAOYSA-N 0.000 description 1
- XFCRCZYNRQHVDP-UHFFFAOYSA-N CC1(C)OB(c2ccc(CO)nc2)OC1(C)C Chemical compound CC1(C)OB(c2ccc(CO)nc2)OC1(C)C XFCRCZYNRQHVDP-UHFFFAOYSA-N 0.000 description 1
- CKSLNKHABBJDCM-BHWOMJMDSA-N CCC(C1)OCC[C@@H]1N(c1c(C(C2=CN(C)[N-]C2)=N2)[o]c3ccc(-c4cncnc4)nc13)C2=O Chemical compound CCC(C1)OCC[C@@H]1N(c1c(C(C2=CN(C)[N-]C2)=N2)[o]c3ccc(-c4cncnc4)nc13)C2=O CKSLNKHABBJDCM-BHWOMJMDSA-N 0.000 description 1
- JBFAYPVVGYCSGS-UHFFFAOYSA-N CCOC(Nc(c1n2)c(C(c(nc3)ccc3OC)=O)[o]c1ccc2OCC)=O Chemical compound CCOC(Nc(c1n2)c(C(c(nc3)ccc3OC)=O)[o]c1ccc2OCC)=O JBFAYPVVGYCSGS-UHFFFAOYSA-N 0.000 description 1
- ZRNKUTOZXNSMHD-UHFFFAOYSA-N CCOc(nc12)ccc1[o]c(C(c(nc1)ccc1OC)=N1)c2NC1=O Chemical compound CCOc(nc12)ccc1[o]c(C(c(nc1)ccc1OC)=N1)c2NC1=O ZRNKUTOZXNSMHD-UHFFFAOYSA-N 0.000 description 1
- NNAOJDFLMHXHOH-DJNXLDHESA-N CC[C@@H](C1)OCCC1N(C(OCC)=O)c1c(C(OCC)=O)[o]c2c1cc(-c1c[n](C)nc1)nc2 Chemical compound CC[C@@H](C1)OCCC1N(C(OCC)=O)c1c(C(OCC)=O)[o]c2c1cc(-c1c[n](C)nc1)nc2 NNAOJDFLMHXHOH-DJNXLDHESA-N 0.000 description 1
- WGNSXDQCODKFJS-STQMWFEESA-N CC[C@@H](C1)OCC[C@@H]1N(c(c1n2)c(C(c3c[n](C)nc3)=N3)[o]c1ccc2Cl)C3=O Chemical compound CC[C@@H](C1)OCC[C@@H]1N(c(c1n2)c(C(c3c[n](C)nc3)=N3)[o]c1ccc2Cl)C3=O WGNSXDQCODKFJS-STQMWFEESA-N 0.000 description 1
- KYFIOKGDIPRPOW-WBUKYKKZSA-N CC[C@@H](C1)OCC[C@@H]1N(c1c(C(/C(/C)=C/N(C)N=C)=N2)[o]c3c1cc(-c1c[n](C)nc1)c(Cl)c3)C2=O Chemical compound CC[C@@H](C1)OCC[C@@H]1N(c1c(C(/C(/C)=C/N(C)N=C)=N2)[o]c3c1cc(-c1c[n](C)nc1)c(Cl)c3)C2=O KYFIOKGDIPRPOW-WBUKYKKZSA-N 0.000 description 1
- NXVZOSLNOCNJFU-HSCFHPFWSA-O CC[C@@H](C1)OCC[C@@H]1N(c1c(C(/C(/C=[NH2+])=C/NC)=N2)[o]c(c(C)c3)c1cc3-c1c[n](C)nc1)C2=O Chemical compound CC[C@@H](C1)OCC[C@@H]1N(c1c(C(/C(/C=[NH2+])=C/NC)=N2)[o]c(c(C)c3)c1cc3-c1c[n](C)nc1)C2=O NXVZOSLNOCNJFU-HSCFHPFWSA-O 0.000 description 1
- CUGGYYBOMIWNEY-ROUUACIJSA-N CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c(cc2)cnc2NC)=N2)[o]c3c1cc(-c1c[n](C)nc1)nc3)C2=O Chemical compound CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c(cc2)cnc2NC)=N2)[o]c3c1cc(-c1c[n](C)nc1)nc3)C2=O CUGGYYBOMIWNEY-ROUUACIJSA-N 0.000 description 1
- GUVUXUQNVPRFCQ-PMACEKPBSA-N CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c(cc3)c1cc3-c1cnccc1)C2=O Chemical compound CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c(cc3)c1cc3-c1cnccc1)C2=O GUVUXUQNVPRFCQ-PMACEKPBSA-N 0.000 description 1
- MYNZFDNRVMDOHX-IRXDYDNUSA-N CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3c1cc(-c1c[n](C)nc1)c(F)c3)C2=O Chemical compound CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3c1cc(-c1c[n](C)nc1)c(F)c3)C2=O MYNZFDNRVMDOHX-IRXDYDNUSA-N 0.000 description 1
- BWTKYKSUROPSHR-PMACEKPBSA-N CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3c1cc(-c1cnccc1)c(C#N)c3)C2=O Chemical compound CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3c1cc(-c1cnccc1)c(C#N)c3)C2=O BWTKYKSUROPSHR-PMACEKPBSA-N 0.000 description 1
- UCEUSYYGJDKMRI-HOTGVXAUSA-N CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3ccc(-[n]4nccc4)nc13)C2=O Chemical compound CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3ccc(-[n]4nccc4)nc13)C2=O UCEUSYYGJDKMRI-HOTGVXAUSA-N 0.000 description 1
- UEGAVSKVQXLELD-GJZGRUSLSA-N CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3ccc(-[n]4ncnc4)nc13)C2=O Chemical compound CC[C@@H](C1)OCC[C@@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3ccc(-[n]4ncnc4)nc13)C2=O UEGAVSKVQXLELD-GJZGRUSLSA-N 0.000 description 1
- UDCSVXIJKDIPHF-QMMMGPOBSA-N CC[C@@H]1OCCC2(CC2)C1 Chemical compound CC[C@@H]1OCCC2(CC2)C1 UDCSVXIJKDIPHF-QMMMGPOBSA-N 0.000 description 1
- XIQCSACWJUJZCL-WPRPVWTQSA-N C[C@@H](C1)[C@]11OCCC2(CC2)C1 Chemical compound C[C@@H](C1)[C@]11OCCC2(CC2)C1 XIQCSACWJUJZCL-WPRPVWTQSA-N 0.000 description 1
- XIQCSACWJUJZCL-HNHGDDPOSA-N C[C@H](C1)C11OCCC2(CC2)C1 Chemical compound C[C@H](C1)C11OCCC2(CC2)C1 XIQCSACWJUJZCL-HNHGDDPOSA-N 0.000 description 1
- KIOKOKYISCAPLD-HALDLXJZSA-N C[C@H](C1)O[C@@H](C)C[C@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3ccc(-c4c[n](C)nc4)nc13)C2=O Chemical compound C[C@H](C1)O[C@@H](C)C[C@H]1N(c1c(C(c2c[n](C)nc2)=N2)[o]c3ccc(-c4c[n](C)nc4)nc13)C2=O KIOKOKYISCAPLD-HALDLXJZSA-N 0.000 description 1
- IXJSDKIJPVSPKF-UHFFFAOYSA-N C[n]1ncc(Br)c1 Chemical compound C[n]1ncc(Br)c1 IXJSDKIJPVSPKF-UHFFFAOYSA-N 0.000 description 1
- NBJYPQMOABEZIF-UHFFFAOYSA-N Cc(c(-c1c[n](C)nc1)c1)cc2c1c(NC(N=C1c3c[n](C)nc3)=O)c1[o]2 Chemical compound Cc(c(-c1c[n](C)nc1)c1)cc2c1c(NC(N=C1c3c[n](C)nc3)=O)c1[o]2 NBJYPQMOABEZIF-UHFFFAOYSA-N 0.000 description 1
- MYUQKYGWKHTRPG-UHFFFAOYSA-N Fc(nc1)ccc1Br Chemical compound Fc(nc1)ccc1Br MYUQKYGWKHTRPG-UHFFFAOYSA-N 0.000 description 1
- ZYLBLRYYAAIKMO-YGPZHTELSA-N N=CCC(C1)[C@@H]1NCC1CC1 Chemical compound N=CCC(C1)[C@@H]1NCC1CC1 ZYLBLRYYAAIKMO-YGPZHTELSA-N 0.000 description 1
- XJBHWDKRZXYEDL-UHFFFAOYSA-N OCCC1OCCCC1 Chemical compound OCCC1OCCCC1 XJBHWDKRZXYEDL-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/14—Ortho-condensed systems
- C07D491/147—Ortho-condensed systems the condensed system containing one ring with oxygen as ring hetero atom and two rings with nitrogen as ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- AIDS & HIV (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161578008P | 2011-12-20 | 2011-12-20 | |
| US61/578,008 | 2011-12-20 | ||
| PCT/CA2012/050909 WO2013091096A1 (en) | 2011-12-20 | 2012-12-19 | Condensed triclyclic compounds as inhibitors of hiv replication |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015500843A JP2015500843A (ja) | 2015-01-08 |
| JP2015500843A5 JP2015500843A5 (enExample) | 2016-02-18 |
| JP6144698B2 true JP6144698B2 (ja) | 2017-06-07 |
Family
ID=48667578
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014547651A Active JP6144698B2 (ja) | 2011-12-20 | 2012-12-19 | Hiv複製の阻害剤としての縮合三環式化合物 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US9399645B2 (enExample) |
| EP (1) | EP2794613B1 (enExample) |
| JP (1) | JP6144698B2 (enExample) |
| WO (1) | WO2013091096A1 (enExample) |
Families Citing this family (107)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013006738A1 (en) | 2011-07-06 | 2013-01-10 | Gilead Sciences, Inc. | Compounds for the treatment of hiv |
| EP3080122B1 (en) | 2013-12-11 | 2018-10-31 | Biogen MA Inc. | Biaryl compounds useful for the treatment of human diseases in oncology, neurology and immunology |
| TW201613916A (en) | 2014-06-03 | 2016-04-16 | Gilead Sciences Inc | TANK-binding kinase inhibitor compounds |
| TW201613936A (en) | 2014-06-20 | 2016-04-16 | Gilead Sciences Inc | Crystalline forms of(2R,5S,13aR)-8-hydroxy-7,9-dioxo-n-(2,4,6-trifluorobenzyl)-2,3,4,5,7,9,13,13a-octahydro-2,5-methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide |
| NO2717902T3 (enExample) | 2014-06-20 | 2018-06-23 | ||
| WO2016036759A1 (en) | 2014-09-04 | 2016-03-10 | Gilead Sciences, Inc. | Methods of treating or preventing hiv in patients using a combination of tenofovir alafenamide and dolutegravir |
| TWI695003B (zh) | 2014-12-23 | 2020-06-01 | 美商基利科學股份有限公司 | 多環胺甲醯基吡啶酮化合物及其醫藥用途 |
| TWI770552B (zh) | 2014-12-24 | 2022-07-11 | 美商基利科學股份有限公司 | 喹唑啉化合物 |
| PT3237397T (pt) | 2014-12-24 | 2019-02-08 | Gilead Sciences Inc | Compostos de isoquinolina para o tratamento de hiv |
| JP6385584B2 (ja) | 2014-12-24 | 2018-09-05 | ギリアード サイエンシーズ, インコーポレイテッド | Hivの処置のための縮合ピリミジン化合物 |
| KR102394917B1 (ko) | 2015-03-04 | 2022-05-09 | 길리애드 사이언시즈, 인코포레이티드 | 톨 유사 수용체 조정제 화합물 |
| SI3466490T1 (sl) | 2015-04-02 | 2020-12-31 | Gilead Sciences, Inc. | Policiklične spojine karbamoilpiridona in njihova farmacevtska uporaba |
| JP2018525412A (ja) | 2015-08-26 | 2018-09-06 | ギリアード サイエンシーズ, インコーポレイテッド | 重水素化トール様受容体調節因子 |
| NZ741785A (en) | 2015-09-30 | 2019-07-26 | Gilead Sciences Inc | 3-cyano-1h-1,2,4-triazol-1-yl compounds and uses thereof for the treatment of hiv |
| CR20180321A (es) | 2015-12-15 | 2018-08-21 | Gilead Sciences Inc | Anticuerpos neutralizadores del virus de inmunodeficiencia humana |
| EP3436434B1 (en) | 2016-03-31 | 2020-07-08 | Oncternal Therapeutics, Inc. | Indoline analogs and uses thereof |
| KR102180740B1 (ko) | 2016-08-19 | 2020-11-20 | 길리애드 사이언시즈, 인코포레이티드 | Hiv 바이러스 감염의 예방적 또는 치유적 치료에 유용한 치료 화합물 |
| WO2018042331A1 (en) | 2016-08-31 | 2018-03-08 | Glaxosmithkline Intellectual Property (No.2) Limited | Combinations and uses and treatments thereof |
| WO2018042332A1 (en) | 2016-08-31 | 2018-03-08 | Glaxosmithkline Intellectual Property (No.2) Limited | Combinations and uses and treatments thereof |
| PT3507276T (pt) | 2016-09-02 | 2022-01-11 | Gilead Sciences Inc | Compostos moduladores do recetor de tipo toll |
| WO2018045150A1 (en) | 2016-09-02 | 2018-03-08 | Gilead Sciences, Inc. | 4,6-diamino-pyrido[3,2-d]pyrimidine derivaties as toll like receptor modulators |
| WO2018051250A1 (en) | 2016-09-14 | 2018-03-22 | Viiv Healthcare Company | Combination comprising tenofovir alafenamide, bictegravir and 3tc |
| WO2018064080A1 (en) | 2016-09-28 | 2018-04-05 | Gilead Sciences, Inc. | Benzothiazol-6-yl acetic acid derivatives and their use for treating hiv infection |
| WO2018081292A1 (en) | 2016-10-27 | 2018-05-03 | Gilead Sciences, Inc. | Crystalline forms of darunavir free base, hydrate, solvates and salts |
| CN106632019B (zh) * | 2016-12-28 | 2019-05-28 | 太原理工大学 | 一种多取代吡啶的制备方法 |
| TWI714820B (zh) | 2017-01-31 | 2021-01-01 | 美商基利科學股份有限公司 | 替諾福韋艾拉酚胺(tenofovir alafenamide)之晶型 |
| JOP20180009A1 (ar) | 2017-02-06 | 2019-01-30 | Gilead Sciences Inc | مركبات مثبط فيروس hiv |
| EP3642229A1 (en) | 2017-06-21 | 2020-04-29 | Gilead Sciences, Inc. | Multispecific antibodies that target hiv gp120 and cd3 |
| US12011506B2 (en) | 2017-06-30 | 2024-06-18 | Viiv Healthcare Company | Combination and uses and treatments thereof |
| PT3661937T (pt) | 2017-08-01 | 2021-09-24 | Gilead Sciences Inc | Formas cristalinas de ((s)-((((2r,5r)-5-(6-amino-9h-purin-9-il)-4-fluoro-2,5-dihidrofurano-2-il)oxi)metil)(fenoxi)fosforil)-l-alaninato de etil (gs-9131) para tratamento de infeções virais |
| AR112412A1 (es) | 2017-08-17 | 2019-10-23 | Gilead Sciences Inc | Formas de sal de colina de un inhibidor de la cápside del vih |
| TWI687415B (zh) | 2017-08-17 | 2020-03-11 | 美商基利科學股份有限公司 | Hiv蛋白質膜抑制劑之固體形式 |
| JOP20180092A1 (ar) | 2017-10-13 | 2019-04-13 | Gilead Sciences Inc | مثبطات hiv بروتياز |
| EP3700573A1 (en) | 2017-10-24 | 2020-09-02 | Gilead Sciences, Inc. | Methods of treating patients co-infected with a virus and tuberculosis |
| AU2018392213B2 (en) | 2017-12-20 | 2021-03-04 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 3'3' cyclic dinucleotides with phosphonate bond activating the STING adaptor protein |
| WO2019123339A1 (en) | 2017-12-20 | 2019-06-27 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 2'3' cyclic dinucleotides with phosphonate bond activating the sting adaptor protein |
| PL3752495T3 (pl) | 2018-02-15 | 2024-01-15 | Gilead Sciences, Inc. | Pochodne pirydynowe i ich zastosowanie do leczenia infekcji hiv |
| CA3175384A1 (en) | 2018-02-16 | 2019-08-22 | Gilead Sciences, Inc. | Methods and intermediates for preparing therapeutic compounds useful in the treatment of retroviridae viral infection |
| TWI833744B (zh) | 2018-04-06 | 2024-03-01 | 捷克科學院有機化學與生物化學研究所 | 3'3'-環二核苷酸 |
| TWI818007B (zh) | 2018-04-06 | 2023-10-11 | 捷克科學院有機化學與生物化學研究所 | 2'3'-環二核苷酸 |
| TW202005654A (zh) | 2018-04-06 | 2020-02-01 | 捷克科學院有機化學與生物化學研究所 | 2,2,─環二核苷酸 |
| TW202014193A (zh) | 2018-05-03 | 2020-04-16 | 捷克科學院有機化學與生物化學研究所 | 包含碳環核苷酸之2’3’-環二核苷酸 |
| US11168130B2 (en) | 2018-07-03 | 2021-11-09 | Gilead Sciences, Inc. | Antibodies that target HIV GP120 and methods of use |
| CN120053445A (zh) | 2018-07-16 | 2025-05-30 | 吉利德科学公司 | 用于治疗hiv的衣壳抑制剂 |
| TWI766172B (zh) | 2018-07-30 | 2022-06-01 | 美商基利科學股份有限公司 | 抗hiv化合物 |
| EP3860717A1 (en) | 2018-10-03 | 2021-08-11 | Gilead Sciences, Inc. | Imidozopyrimidine derivatives |
| TWI721624B (zh) | 2018-10-31 | 2021-03-11 | 美商基利科學股份有限公司 | 經取代之6-氮雜苯并咪唑化合物 |
| CA3117556A1 (en) | 2018-10-31 | 2020-05-07 | Gilead Sciences, Inc. | Substituted 6-azabenzimidazole compounds as hpk1 inhibitors |
| WO2020176505A1 (en) | 2019-02-25 | 2020-09-03 | Gilead Sciences, Inc. | Protein kinase c agonists |
| WO2020176510A1 (en) | 2019-02-25 | 2020-09-03 | Gilead Sciences, Inc. | Protein kinase c agonists |
| EP3935065A1 (en) | 2019-03-07 | 2022-01-12 | Institute of Organic Chemistry and Biochemistry ASCR, V.V.I. | 3'3'-cyclic dinucleotide analogue comprising a cyclopentanyl modified nucleotide as sting modulator |
| JP7350871B2 (ja) | 2019-03-07 | 2023-09-26 | インスティチュート オブ オーガニック ケミストリー アンド バイオケミストリー エーエスシーアール,ヴイ.ヴイ.アイ. | 2’3’-環状ジヌクレオチドおよびそのプロドラッグ |
| WO2020178770A1 (en) | 2019-03-07 | 2020-09-10 | Institute Of Organic Chemistry And Biochemistry Ascr, V.V.I. | 3'3'-cyclic dinucleotides and prodrugs thereof |
| HUE059677T2 (hu) | 2019-03-22 | 2022-12-28 | Gilead Sciences Inc | Áthidalt triciklusos karbamoilpiridon-vegyületek és ezek gyógyszerészeti alkalmazása |
| TW202104210A (zh) | 2019-04-17 | 2021-02-01 | 美商基利科學股份有限公司 | Hiv蛋白酶抑制劑 |
| WO2020214647A1 (en) | 2019-04-17 | 2020-10-22 | Gilead Sciences, Inc. | Solid forms of an hiv protease inhibitor |
| TWI751517B (zh) | 2019-04-17 | 2022-01-01 | 美商基利科學股份有限公司 | 類鐸受體調節劑之固體形式 |
| TW202210480A (zh) | 2019-04-17 | 2022-03-16 | 美商基利科學股份有限公司 | 類鐸受體調節劑之固體形式 |
| CN111848443A (zh) * | 2019-04-29 | 2020-10-30 | 南通泰禾化工股份有限公司 | 一种水杨腈的制备方法 |
| TWI762925B (zh) | 2019-05-21 | 2022-05-01 | 美商基利科學股份有限公司 | 鑑別對使用gp120 v3聚醣導向之抗體的治療敏感之hiv病患的方法 |
| EP3972695A1 (en) | 2019-05-23 | 2022-03-30 | Gilead Sciences, Inc. | Substituted exo-methylene-oxindoles which are hpk1/map4k1 inhibitors |
| RU2717101C1 (ru) | 2019-06-03 | 2020-03-18 | Андрей Александрович Иващенко | Анелированные 9-гидрокси-1,8-диоксо-1,3,4,8-тетрагидро-2Н-пиридо[1,2-a]пиразин-7-карбоксамиды - ингибиторы интегразы ВИЧ, способы их получения и применения |
| CA3140708A1 (en) | 2019-06-18 | 2020-12-24 | Helen Horton | Combination of hepatitis b virus (hbv) vaccines and pyridopyrimidine derivatives |
| CN114245807B (zh) | 2019-06-25 | 2025-05-02 | 吉利德科学公司 | Flt3l-fc融合蛋白和使用方法 |
| KR20220047277A (ko) | 2019-07-16 | 2022-04-15 | 길리애드 사이언시즈, 인코포레이티드 | Hiv 백신, 및 이의 제조 및 사용 방법 |
| US20220257619A1 (en) | 2019-07-18 | 2022-08-18 | Gilead Sciences, Inc. | Long-acting formulations of tenofovir alafenamide |
| EP4017476A1 (en) | 2019-08-19 | 2022-06-29 | Gilead Sciences, Inc. | Pharmaceutical formulations of tenofovir alafenamide |
| EP4643882A2 (en) | 2019-11-26 | 2025-11-05 | Gilead Sciences, Inc. | Capsid inhibitors for the prevention of hiv |
| MX2022007930A (es) | 2019-12-24 | 2022-08-08 | Carna Biosciences Inc | Compuestos moduladores de diacilglicerol quinasa. |
| CR20220418A (es) | 2020-02-24 | 2022-10-10 | Gilead Sciences Inc | Compuestos tetracíclicos para el tratamiento de infecciones por vih |
| WO2021188959A1 (en) | 2020-03-20 | 2021-09-23 | Gilead Sciences, Inc. | Prodrugs of 4'-c-substituted-2-halo-2'-deoxyadenosine nucleosides and methods of making and using the same |
| CN111548349A (zh) * | 2020-05-13 | 2020-08-18 | 厦门云凡医药科技有限公司 | 一种ret激酶抑制剂中间体及其制备方法 |
| EP4153181A1 (en) | 2020-05-21 | 2023-03-29 | Gilead Sciences, Inc. | Pharmaceutical compositions comprising bictegravir |
| WO2021262990A1 (en) | 2020-06-25 | 2021-12-30 | Gilead Sciences, Inc. | Capsid inhibitors for the treatment of hiv |
| BR112023002164A2 (pt) | 2020-08-07 | 2023-03-14 | Gilead Sciences Inc | Profármacos de análogos de nucleotídeos de fosfonamida e seu uso farmacêutico |
| JP7691494B2 (ja) | 2020-09-30 | 2025-06-11 | ギリアード サイエンシーズ, インコーポレイテッド | 架橋三環式カルバモイルピリドン化合物及びその使用 |
| TWI815194B (zh) | 2020-10-22 | 2023-09-11 | 美商基利科學股份有限公司 | 介白素2-Fc融合蛋白及使用方法 |
| CA3195799A1 (en) | 2020-11-11 | 2022-05-19 | Stephen R. Martin | Methods of identifying hiv patients sensitive to therapy with gp120 cd4 binding site-directed antibodies |
| LT4196479T (lt) | 2021-01-19 | 2023-12-11 | Gilead Sciences, Inc. | Pakeistieji piridotriazino junginiai ir jų panaudojimo būdai |
| TW202313094A (zh) | 2021-05-18 | 2023-04-01 | 美商基利科學股份有限公司 | 使用FLT3L—Fc融合蛋白之方法 |
| JP7686091B2 (ja) | 2021-06-23 | 2025-05-30 | ギリアード サイエンシーズ, インコーポレイテッド | ジアシルグリセロールキナーゼ調節化合物 |
| EP4359389A1 (en) | 2021-06-23 | 2024-05-01 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
| AU2022298639C1 (en) | 2021-06-23 | 2025-07-17 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
| CA3222277A1 (en) | 2021-06-23 | 2022-12-29 | Gilead Sciences, Inc. | Diacylglyercol kinase modulating compounds |
| JP7736929B2 (ja) | 2021-12-03 | 2025-09-09 | ギリアード サイエンシーズ, インコーポレイテッド | Hivウイルス感染症のための治療化合物 |
| US12084467B2 (en) | 2021-12-03 | 2024-09-10 | Gilead Sciences, Inc. | Therapeutic compounds for HIV virus infection |
| EP4440702B1 (en) | 2021-12-03 | 2025-05-21 | Gilead Sciences, Inc. | Therapeutic compounds for hiv virus infection |
| TWI843506B (zh) | 2022-04-06 | 2024-05-21 | 美商基利科學股份有限公司 | 橋聯三環胺甲醯基吡啶酮化合物及其用途 |
| WO2024006982A1 (en) | 2022-07-01 | 2024-01-04 | Gilead Sciences, Inc. | Therapeutic compounds useful for the prophylactic or therapeutic treatment of an hiv virus infection |
| AU2023307100A1 (en) | 2022-07-12 | 2025-01-02 | Gilead Sciences, Inc. | Hiv immunogenic polypeptides and vaccines and uses thereof |
| US20240083984A1 (en) | 2022-08-26 | 2024-03-14 | Gilead Sciences, Inc. | Dosing and scheduling regimen for broadly neutralizing antibodies |
| US20240226130A1 (en) | 2022-10-04 | 2024-07-11 | Gilead Sciences, Inc. | 4'-thionucleoside analogues and their pharmaceutical use |
| AR132464A1 (es) | 2023-04-19 | 2025-07-02 | Gilead Sciences Inc | Régimen de dosificación de inhibidor de la cápside |
| TW202448483A (zh) | 2023-05-31 | 2024-12-16 | 美商基利科學股份有限公司 | 用於hiv之治療性化合物 |
| WO2024249517A1 (en) | 2023-05-31 | 2024-12-05 | Gilead Sciences, Inc. | Anti-hiv compounds |
| WO2024249573A1 (en) | 2023-05-31 | 2024-12-05 | Gilead Sciences, Inc. | Solid forms of compounds useful in the treatment of hiv |
| WO2025029247A1 (en) | 2023-07-28 | 2025-02-06 | Gilead Sciences, Inc. | Weekly regimen of lenacapavir for the treatment and prevention of hiv |
| WO2025042394A1 (en) | 2023-08-23 | 2025-02-27 | Gilead Sciences, Inc. | Dosing regimen of hiv capsid inhibitor |
| WO2025076542A1 (en) | 2023-10-05 | 2025-04-10 | Jones R Brad | Atovaquone as an ros inducer for use in the elimination of hiv-infected t-cells |
| TW202515549A (zh) | 2023-10-11 | 2025-04-16 | 美商基利科學股份有限公司 | 橋聯三環胺甲醯基吡啶酮化合物及其用途 |
| TW202530226A (zh) | 2023-10-11 | 2025-08-01 | 美商基利科學股份有限公司 | 橋聯三環胺甲醯基吡啶酮化合物及其用途 |
| WO2025080863A1 (en) | 2023-10-11 | 2025-04-17 | Gilead Sciences, Inc. | Bridged tricyclic carbamoylpyridone compounds and uses thereof |
| WO2025137245A1 (en) | 2023-12-22 | 2025-06-26 | Gilead Sciences, Inc. | Solid forms of hiv integrase inhibitors |
| US20250333424A1 (en) | 2024-03-01 | 2025-10-30 | Gilead Sciences, Inc. | Antiviral compounds |
| WO2025184447A1 (en) | 2024-03-01 | 2025-09-04 | Gilead Sciences, Inc. | Pharmaceutical compositions comprising hiv integrase inhibitors |
| US20250289822A1 (en) | 2024-03-01 | 2025-09-18 | Gilead Sciences, Inc. | Solid forms of hiv integrase inhibitors |
| WO2025212814A1 (en) | 2024-04-03 | 2025-10-09 | Gilead Sciences, Inc. | Anti-hiv compounds |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7642277B2 (en) | 2002-12-04 | 2010-01-05 | Boehringer Ingelheim International Gmbh | Non-nucleoside reverse transcriptase inhibitors |
| EP1998769A2 (en) | 2006-02-03 | 2008-12-10 | Tibotec Pharmaceuticals Ltd. | Treating hiv infection, wherein hiv has a k65r mutation |
| CA2758149A1 (en) | 2009-04-09 | 2010-10-14 | Boehringer Ingelheim International Gmbh | Inhibitors of hiv replication |
-
2012
- 2012-12-19 WO PCT/CA2012/050909 patent/WO2013091096A1/en not_active Ceased
- 2012-12-19 EP EP12860305.7A patent/EP2794613B1/en active Active
- 2012-12-19 US US14/366,421 patent/US9399645B2/en active Active
- 2012-12-19 JP JP2014547651A patent/JP6144698B2/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| US20150011531A1 (en) | 2015-01-08 |
| EP2794613A1 (en) | 2014-10-29 |
| EP2794613B1 (en) | 2017-03-29 |
| EP2794613A4 (en) | 2015-05-27 |
| WO2013091096A1 (en) | 2013-06-27 |
| JP2015500843A (ja) | 2015-01-08 |
| US9399645B2 (en) | 2016-07-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP6144698B2 (ja) | Hiv複製の阻害剤としての縮合三環式化合物 | |
| TWI858008B (zh) | 免疫調節劑、藥物組合物及其應用 | |
| US11529341B2 (en) | Bicyclic compounds as inhibitors of PD1/PD-L1 interaction/activation | |
| CN109952300B (zh) | 5或8-取代的咪唑并[1,5-a]吡啶 | |
| US20100227880A1 (en) | Chemical compounds | |
| JP7451765B2 (ja) | Cdk阻害剤としてのピリジンアセトアミド系誘導体、その調製方法及び用途 | |
| US10202389B2 (en) | Pyrazolopyrimidinyl inhibitors of ubiquitin-activating enzyme | |
| JP6786566B2 (ja) | ヘテロアリール化合物及びその使用方法 | |
| JP7592748B2 (ja) | 抗ウイルス1,3-ジ-オキソ-インデン化合物 | |
| JP2022502444A (ja) | 3−アザビシクロ[3,1,1]ヘプタン誘導体及びこれを含む薬学的組成物 | |
| US20240317758A1 (en) | Nek7 inhibitors | |
| TWI823420B (zh) | 用作cdk激酶抑制劑的化合物及其應用 | |
| JP2020143161A (ja) | CaMKII阻害剤及びその使用 | |
| WO2022092141A1 (ja) | 抗ウイルス活性を有するアミド誘導体 | |
| CN120590351A (zh) | 抗病毒素1,3-二氧代茚化合物 | |
| JP7605446B2 (ja) | ベンゾトリアゾール化合物 | |
| KR102894005B1 (ko) | 항바이러스 1,3-다이-옥소-인덴 화합물 | |
| JP2025521097A (ja) | Lrrk2阻害剤 | |
| TWI692476B (zh) | 環丁基-咪唑啶酮化合物 | |
| WO2025096981A1 (en) | Modulators of dcn-1 and methods of use thereof | |
| CN119546607A (zh) | Lrrk2抑制剂 | |
| EP4638448A1 (en) | Conjugates comprising antifungals and casein kinase (ck1) inhibitors and methods of use thereof | |
| TW202317093A (zh) | 具有hiv複製抑制作用之縮合雜環衍生物 | |
| HK40003408A (en) | 5 or 8-SUBSTITUTED IMIDAZO [1, 5-A] PYRIDINES | |
| HK40003408B (en) | 5 or 8-SUBSTITUTED IMIDAZO [1, 5-A] PYRIDINES |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20151218 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20151218 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20160721 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20160808 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20161107 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20161207 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20170306 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20170412 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20170511 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 6144698 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |